Structure of PDB 6cod Chain A Binding Site BS01
Receptor Information
>6cod Chain A (length=259) Species:
3702
(Arabidopsis thaliana) [
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MERKHHFVLVHNACHGAWIWYKLKPLLESAGHRVTAVELAASGIDPRPIQ
AVETVDEYSKPLIETLKSLPENEEVILVGFSFGGINIALAADIFPAKIKV
LVFLNAFLPDTTHVPSHVLDKLMEMFGGWGDTEFSSHETRNGTMSLLKMG
PKFMKARLYQNCPIEDYELAKMLHRQGSFFTEDLSKKEKFSEEGYGSVQR
VYVMSSEDKIIPCDFIRWMIDNFNVSKVYEIDGGDHMVMLSKPQKLFDSL
SAIATDYMG
Ligand information
Ligand ID
HBX
InChI
InChI=1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H
InChIKey
HUMNYLRZRPPJDN-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
O=Cc1ccccc1
OpenEye OEToolkits 1.5.0
c1ccc(cc1)C=O
Formula
C7 H6 O
Name
benzaldehyde
ChEMBL
CHEMBL15972
DrugBank
ZINC
ZINC000000895145
PDB chain
6cod Chain A Residue 304 [
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Receptor-Ligand Complex Structure
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PDB
6cod
AtHNL enantioselectivity mutants
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
N12 S81 W129 L147 M149 H236
Binding residue
(residue number reindexed from 1)
N12 S81 W129 L147 M149 H236
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
N12 S81 F82 D208 H236 M237
Catalytic site (residue number reindexed from 1)
N12 S81 F82 D208 H236 M237
Enzyme Commision number
4.1.2.10
: (R)-mandelonitrile lyase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0016829
lyase activity
GO:0046593
mandelonitrile lyase activity
Biological Process
GO:0009611
response to wounding
GO:0016139
glycoside catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6cod
,
PDBe:6cod
,
PDBj:6cod
PDBsum
6cod
PubMed
UniProt
Q9LFT6
|HNL_ARATH Alpha-hydroxynitrile lyase (Gene Name=HNL)
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